Join a multidisciplinary team pushing the boundaries of pharmaceutical innovation, from molecular discovery to global patient impact. Shape the future of medicine at Zenth Pharma.
Lead AI-driven molecular modeling for our oncology pipeline. Collaborate with cross-functional teams to accelerate hit-to-lead optimization.
Monitor Phase II/III trials across North America. Ensure GCP compliance, data integrity, and subject safety in immuno-oncology programs.
Bridge lab-scale synthesis to commercial GMP manufacturing. Optimize yield, purity, and process robustness for biologics and small molecules.
Design global regulatory pathways for novel modalities. Interface with FDA, EMA, and PMAs to secure accelerated approvals.
Serve as the scientific bridge between Zenth Pharma and key opinion leaders. Support clinical development with real-world evidence and insights.
Design statistical analysis plans, author CSRs, and ensure compliance with ICH E9 guidelines. Mentor junior statisticians across trials.
We invest in our people because breakthroughs require both brilliant minds and sustained support.
Work with state-of-the-art labs, AI modeling platforms, and early-access clinical data across all therapeutic areas.
Transfer across our Basel, Boston, Singapore, or Cambridge sites. Cultural immersion + relocation support.
Competitive base salary, annual bonuses, RSUs, and milestone-based commercialization equity.
Comprehensive medical/dental/vision, mental health stipends, parental leave, and flexible PTO.
Transparent, efficient, and designed to respect your time while ensuring scientific and cultural alignment.
Submit your CV and brief motivation. HR conducts a 20-minute alignment call within 5 business days.
Role-specific challenge: coding, data analysis, regulatory mock submission, or case study.
Meet your future team, functional lead, and cross-divisional stakeholders. 2 rounds max.
Transparent compensation breakdown, equity timeline, and 30-60-90 day ramp plan.